NAPROXEN

Product NDC
53943-144
Type
HUMAN OTC DRUG
Nonproprietary name
NAPROXEN SODIUM
Dosage form
TABLET, COATED
Route
ORAL
Labeler
DISCOUNT DRUG MART
Application
ANDA079096
Marketing category
ANDA
Substance
NAPROXEN SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
53943-144-021 BOTTLE, PLASTIC in 1 CARTON (53943-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC2014-10-28NoHistorical
53943-144-031 BOTTLE, PLASTIC in 1 CARTON (53943-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC2014-10-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1144-DDM-2025-0515DISCOUNT DRUG MART2025-05-15HUMAN OTC DRUG LABEL3